CD44 CD44 molecule (IN blood group)
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 28 |
Likely benign | 0 | 28 |
association | 0 | 24 |
not provided | 76 | 0 |
Uncertain significance | 0 | 62 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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4 |
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112 |
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26 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Filtering | : |
Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | CDW44 |
SYNONYM | CSPG8 |
SYNONYM | ECM-III |
SYNONYM | ECMR-III |
SYNONYM | H-CAM |
SYNONYM | HCELL |
SYNONYM | HUTCH-1 |
SYNONYM | HUTCH-I |
SYNONYM | Hermes-1 |
SYNONYM | IN |
SYNONYM | LHR |
SYNONYM | MC56 |
SYNONYM | MDU2 |
SYNONYM | MDU3 |
SYNONYM | MIC4 |
SYNONYM | Pgp1 |
MIM | 107269 OMIM |
HGNC | HGNC:1681 HGNC |
Ensembl | ENSG00000026508 Ensembl |
AllianceGenome | HGNC:1681 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000278386.10 | hg38 | chr11 | 35,139,286 | 35,229,333 | 90,048 |
ENST00000526025.2 | hg38 | chr11 | 35,138,882 | 35,177,110 | 38,229 |
ENST00000352818.8 | hg38 | chr11 | 35,139,304 | 35,229,333 | 90,030 |
ENST00000434472.6 | hg38 | chr11 | 35,139,293 | 35,229,666 | 90,374 |
ENST00000433892.6 | hg38 | chr11 | 35,139,188 | 35,230,027 | 90,840 |
ENST00000263398.11 | hg38 | chr11 | 35,139,171 | 35,232,402 | 93,232 |
ENST00000428726.8 | hg38 | chr11 | 35,139,171 | 35,232,402 | 93,232 |
ENST00000526669.6 | hg38 | chr11 | 35,139,182 | 35,229,460 | 90,279 |
ENST00000415148.6 | hg38 | chr11 | 35,139,170 | 35,229,468 | 90,299 |
ENST00000415148.6 | hg19 | chr11 | 35,160,717 | 35,251,015 | 90,299 |
ENST00000263398.11 | hg19 | chr11 | 35,160,718 | 35,253,949 | 93,232 |
ENST00000428726.8 | hg19 | chr11 | 35,160,718 | 35,253,949 | 93,232 |
ENST00000433892.6 | hg19 | chr11 | 35,160,735 | 35,251,574 | 90,840 |
ENST00000526025.2 | hg19 | chr11 | 35,160,429 | 35,198,657 | 38,229 |
ENST00000278386.10 | hg19 | chr11 | 35,160,833 | 35,250,880 | 90,048 |
ENST00000434472.6 | hg19 | chr11 | 35,160,840 | 35,251,213 | 90,374 |
ENST00000352818.8 | hg19 | chr11 | 35,160,851 | 35,250,880 | 90,030 |
ENST00000526669.6 | hg19 | chr11 | 35,160,729 | 35,251,007 | 90,279 |
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